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Effect of continuous recombinant human endostatin pumping combined with TP chemotherapy on serum malignant molecules and angiogenesis molecules in patients with advanced ovarian cancer

机译:连续重组人内皮抑素联合TP化疗对晚期卵巢癌患者血清恶性分子和血管生成分子的影响

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Objective:To study the effect of continuous recombinant human endostatin pumping combined with TP chemotherapy on serum malignant molecules and angiogenesis molecules in patients with advanced ovarian cancer.Methods:78 patients with advanced ovarian cancer who were treated in our hospital between July 2011 and December 2015 were selected and divided into observation group and control group (n=39) according to the single-blind randomized control method. Before treatment and after 4 cycles of treatment, electrochemical luminescence immunity analyzer was used to detect serum tumor marker levels;RIA method was used to determine serum apoptosis molecule levels;enzyme-linked immunosorbent assay (ELISA) was used to detect the serum angiogenesis molecule levels.Results:Before treatment, differences in serum levels of tumor markers, apoptosis molecules and angiogenesis molecules were not statistically significant between two groups of patients (P>0.05). After 4 cycles of treatment, serum carbohydrate antigen 125 (CA125), carbohydrate antigen 153 (CA153), human epididymis protein 4 (HE4), carcinoembryonic antigen (CEA), human chorionic gonadotropin (β-HCG), Bcl-2, Survivin, Bag-1, angiogenin-2 (Ang-2), vascular endothelial growth factor (VEGF) and basic fibroblast growth factor (bFGF) levels of observation group were significantly lower than those of control group (P<0.05) while Bax level was significantly higher than that of control group (P<0.05).Conclusions:Continuous recombinant human endostatin pumping combined with TP chemotherapy can decrease the malignant degree of advanced ovarian cancer and inhibit angiogenesis.
机译:目的:研究连续性重组人内皮抑素联合TP化疗对晚期卵巢癌患者血清恶性分子和血管生成分子的影响。方法:2011年7月至2015年12月在我院接受治疗的78例晚期卵巢癌患者根据单盲随机对照方法,选择观察组和对照组(n = 39)。治疗前及治疗4个疗程后,采用电化学发光免疫分析仪检测血清肿瘤标志物水平; RIA法测定血清细胞凋亡分子水平;酶联免疫吸附法(ELISA)检测血清血管生成分子水平。结果:治疗前,两组患者血清肿瘤标志物,凋亡分子和血管生成分子水平差异无统计学意义(P> 0.05)。治疗4个周期后,血清碳水化合物抗原125(CA125),碳水化合物抗原153(CA153),人附睾蛋白4(HE4),癌胚抗原(CEA),人绒毛膜促性腺激素(β-HCG),Bcl-2,Survivin,观察组Bag-1,血管生成素-2(Ang-2),血管内皮生长因子(VEGF)和碱性成纤维细胞生长因子(bFGF)水平明显低于对照组(P <0.05),而Bax水平显着低于对照组。结论:连续重组人内皮抑素联合TP化疗可降低晚期卵巢癌的恶性程度,抑制血管生成。

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